Prebreeding moult, plumage and evidence for a presupplemental moult in the Great Knot Calidris tenuirostris

被引:13
作者
Battley, PF
Rogers, DI
Hassell, CJ
机构
[1] Griffith Univ, Australian Sch Environm Studies, Nathan, Qld 4111, Australia
[2] Charles Sturt Univ, Sch Environm & Informat Sci, Albury, NSW 2640, Australia
关键词
D O I
10.1111/j.1474-919X.2006.00469.x
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
We studied the prebreeding moult and resulting plumage in a long-distance migrant sandpiper (Scolopacidae), the Great Knot Calidris tenuirostris, on the non-breeding grounds (northwest Australia), on arrival at the staging grounds after the first migratory flight (eastern China) and on or near the Russian breeding grounds (Russian data from museum specimens). We show that breeding plumage scores and breast blackness were affected not only by the increase in moulted feathers but also in the wearing down of overlaying pale tips of fresh feathers. Birds migrating from Australia and arriving in China had completed or suspended moult, but more moult must occur in Asia as Russian specimens had moulted more of their mantle and scapular feathers. Russian birds had significantly more red feathering on their upperparts than had birds in Australia or those arriving in China. The increase in reddish feathers cannot by accounted for simply by continuation of the prealternate moult. Instead, a third, presupplemental moult must occur, in which red-marked feathers replace some scapular and especially mantle feathers that were acquired in a prealternate moult only 1-3 months earlier. Great Knot sexes show little size and plumage dimorphism, whereas two other sandpipers that have supplemental plumages (Ruff Philomachus pugnax and Bar-tailed Godwit Limosa lapponica) are thought to be highly sexually selected. Bidirectional sexual selection may therefore be involved in the evolution of a supplemental plumage in Great Knots.
引用
收藏
页码:27 / 38
页数:12
相关论文
共 27 条
[1]   Molecular vs. phenotypic sexing in Red Knots [J].
Baker, AJ ;
Piersma, T .
CONDOR, 1999, 101 (04) :887-893
[2]  
Barter M. A., 2000, STILT, V37, P13
[3]   Do body condition and plumage during fuelling predict northwards departure dates of Great Knots Calidris tenuirostris from north-west Australia? [J].
Battley, PF ;
Piersma, T ;
Rogers, DI ;
Dekinga, A ;
Spaans, B ;
Van Gils, JA .
IBIS, 2004, 146 (01) :46-60
[4]   Empirical evidence for differential organ reductions during trans-oceanic bird flight [J].
Battley, PF ;
Piersma, T ;
Dietz, MW ;
Tang, SX ;
Dekinga, A ;
Hulsman, K .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2000, 267 (1439) :191-195
[5]   Is long-distance bird flight equivalent to a high-energy fast? Body composition changes in freely migrating and captive fasting great knots [J].
Battley, PF ;
Dietz, MW ;
Piersma, T ;
Dekinga, A ;
Tang, SX ;
Hulsman, K .
PHYSIOLOGICAL AND BIOCHEMICAL ZOOLOGY, 2001, 74 (03) :435-449
[6]   Wing molt and assortative mating in common terns: A test of the molt-signaling hypothesis [J].
Bridge, ES ;
Nisbet, ICT .
CONDOR, 2004, 106 (02) :336-343
[7]  
Byrkjedal I., 1998, TUNDRA PLOVERS EURAS
[8]  
Higgins P, 1996, Handbook of Australian, New Zealand and Antarctic birds. Volume 3: snipe to pigeons., V3
[9]   The first basic problem: A review of molt and plumage homologies [J].
Howell, SNG ;
Corben, C ;
Pyle, P ;
Rogers, DI .
CONDOR, 2003, 105 (04) :635-653
[10]  
HUMPHREY PHILIP S., 1959, AUK, V76, P1